Cytarabine conjugates for cancer therapy

ABSTRACT

The present invention relates to conjugates comprising cytarabine and an amino acid for use in the treatment of cancer. In particular, the present invention relates to conjugates of cytarabine and aspartic acid for use in the treatment of hematological cancers.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a Continuation-in-Part of U.S. application Ser. No. 15/780,732, filed on Jun. 1, 2018, which is a National Phase entry of PCT International Application Serial No. PCT/IL2016/050077, filed on Jan. 25, 2016, claiming the benefit of U.S. Ser. No. 62/262,428, filed on Dec. 3, 2015, which are incorporated in their entirety herein by reference.

FIELD OF THE INVENTION

The present invention relates to conjugates comprising cytarabine and an amino acid for use in the treatment of cancer. In particular, the present invention relates to conjugates of cytarabine and aspartic acid for use in the treatment of hematological cancers.

BACKGROUND OF THE INVENTION Anti-Proliferative Drugs

Anti-proliferative drugs, also known as anti-metabolites, anti-neoplastic agents or covalent DNA binding drugs, act by inhibiting essential metabolic pathways and are commonly used in the treatment of malignant diseases. However, their high toxicity to normal cells and severe side effects limit their use as therapeutic agents. Undesirable side effects include anemia, emesis and balding due to cytotoxic effects on rapidly dividing normal cells, such as stem cells in the bone marrow, epithelial cells of the intestinal tract, hair follicle cells, etc.

Another major problem associated with anti-proliferative drugs is inherent or acquired resistance of tumors to the drugs. For example, although the initial remission rate following treatment with L-asparaginase is quite high in acute lymphoblastic leukemia (ALL) patients, relapse and associated drug resistance pose a significant clinical problem. Studies have demonstrated increased asparagine synthetase (AS) expression in asparaginase-resistant cells, which has led to the hypothesis that elevated AS activity permits drug-resistant survival of malignant cells.

Nucleotide/Nucleoside Analogs

Nucleoside analogs compete with their physiologic counterparts for incorporation into nucleic acids and have earned an important place in the treatment of acute leukemia. The most important of these are the arabinose nucleosides; a unique class of antimetabolites originally isolated from the sponge Cryptothethya crypta, but now produced synthetically. They differ from the physiologic deoxyribonucleosides by the presence of a 2′—OH group in the cis configuration relative to the N-glycosyl bond between cytosine and arabinoside sugar. Several arabinose nucleosides have useful antitumor and antiviral effects. The most active cytotoxic agent of this class is cytosine arabinoside (cytarabine or ara-C). Cytarabine is currently used for treating cancers of white blood cells such as Acute Myeloid Leukemia (AML), Acute Lymphoblastic Leukemia (ALL), Chronic Myeloid Leukemia (CML), Chronic Lymphoblastic Leukemia (CLL), and Myelodysplastic Syndromes (MDS). However, cytarabine is highly toxic having severe side-effects such as cerebellar toxicity and bone marrow suppression. Cytarabine treatment is therefore limited, and often restricted, in elderly patients and in patients having hepatic, renal, or cerebellar dysfunction.

One objective of analog development in the area of cytidine antimetabolites has been to find compounds that preserve the inhibitory activity of ara-C but are resistant to deamination. A number of deaminase-resistant analogs have been developed, including cyclo-cytidine (Ho DHW, 1974) and N⁴-behenoyl ara-C (Kodama et al., 1989) that showed anti-leukemic activity in some clinical trials, but had undesirable side effects (Woodcock et al., 1980). Other representative compounds are N⁴-Palmitoyl-ara-C, 2′-Azido-2′-deoxy ara-C, 5′-(Cortisone 21-phosphoryl) ester of ara-C, 5′-Acyl esters of ara-C (e.g., 5′-palmitate ester), N⁴Behenoyl-ara-C, ara-C conjugate with poly-H⁵ (2-hydroxyethyl)-L-glutamine, Dihydro-5-azacytidine, 5-Aza-arabinosylcytosine, 5-Aza 2′-deoxycytidine and 2′-2′-Difluorodeoxycytidine (Hertel et al., 1990 and Heinemann et al., 1988).

Gemcitabine (2,2-difluorodeoxycytidine, dFdC) is the most important cytidine analog to enter clinical trials since ara-C. It has become incorporated into the standard first-line therapy for patients with pancreatic cancer, lung cancer, and transitional cell cancer of the bladder.

Nucleotide analogs have also been used in non-cancer applications. For example Flucytosine, a fluorinated cytosine analog, is used as an antifungal agent.

Amino Acids and Proliferative Disease

Asparagine is a non-essential amino acid that is required by rapidly proliferating cells. Mammalian cells can synthesize asparagine from aspartate using the ATP-dependent enzyme asparagine synthetase (EC 6.3.5.4), which transfers the amino group from the amide of glutamine to the β-carboxyl of aspartate in a reaction that can be represented as: Glutamine+Aspartate+ATP+H₂O=Glutamate+Asparagine+AMP+PPi.

Malignant cells often require higher amounts of amino acids, including asparagine, to support their metabolism and proliferation. In order to fulfill the need for high amounts of amino acids, malignant cells develop the ability to actively transport amino acids from their environment. Moreover, asparagine synthetase deficiency occurs in certain tumors, causing them to rely on an external supply of asparagine from other sources, such as serum. This observation led to the development of the enzyme L-asparaginase (CE 3.5.1.1) as a chemotherapeutic agent. L-asparaginase hydrolyzes L-asparagine to aspartate and ammonia, hence depleting L-asparagine from the serum and inhibiting tumor growth. L-asparaginase is used mainly in the treatment of Acute Lymphoblastic Leukemia (ALL) and shows some activity against other hematological cancers including acute non-lymphocytic leukemia.

The L-asparaginase used in the clinic is available in two unmodified (native) forms purified from bacterial sources, and one as a PEGylated compound. U.S. Pat. No. 4,179,337 teaches PEGylated L-asparaginase, wherein the enzyme is coupled to PEG having a molecular weight of about 500 to 20,000 Daltons.

The in vivo down-regulation of asparagine synthetase may provide an efficient mechanism for inhibiting tumor growth. However, cells respond to amino acid deprivation by a concerted increase in asparagine synthetase mRNA, protein, and enzymatic activity that involves transcriptional control of the asparagine synthetase gene.

A metabolic approach was initially used to inhibit the activity of asparagine synthetase by the generation of L-asparagine and L-aspartic acid analogs. Analogs including 5-carboxamido-4-amino-3-isoxazolidone (Stammer et al., 1978) and N-substituted sulfonamides and N′-substituted sulfonylhydrazides have been prepared as sulfur analogues of L-asparagine (Brynes S et al., 1978a; Brynes S et al., 1978b). U.S. Pat. No. 4,348,522 teaches the salt of PALA, N-phosphonacetyl-L-aspartic acid, which has been shown to exhibit anti-tumor activity and is presently in clinical trials as combination chemotherapy for colorectal and pancreatic cancers.

Aspartic acid-ara-C was used as a raw material for the synthesis of peptide T-ara-C conjugates for targeting CD4 positive cells (Manfredini et al., 2000).

The use of prodrugs to impart desired characteristics such as increased bioavailability or increased site-specificity is a recognized concept in the art of pharmaceutical development. For example, direct or indirect conjugation of a drug to an antibody creates a stable conjugate that can arrive at the target site with minimum dissociation of the drug. Drug targeting may be combined with a mechanism of selective release of the drug for maximal potency.

U.S. Pat. No. 4,296,105 describes doxorubicin derivatives linked to an optionally substituted amino acid at the hydroxy group of the amino acid residue, which possess in vitro a higher antitumor activity and lower toxicity than doxorubicin.

U.S. Pat. No. 5,962,216 teaches tumor activated prodrugs which are unable to enter the cell until cleaved by a factor or factors secreted by a target cell.

U.S. Pat. No. 5,650,386 teaches compositions comprising at least one active agent, and at least one modified non-alpha amino acid or poly amino acid, which acts as a carrier of the active agent. The amino acid modification includes acylation or sulfonation of at least one free amine group.

U.S. Pat. Nos. 6,623,731; 6,428,780 and 6,344,213 teach non-covalent mixtures comprising modified amino acids as carriers for biologically active agents.

U.S. Pat. No. 5,106,951 discloses a conjugate comprising an aromatic drug non-covalently intercalated between two aromatic side chains on an oligopeptide, and an antibody or antibody fragment covalently attached to the oligopeptide for targeting to cancer cells.

U.S. Pat. No. 6,617,306 teaches a carrier for the in vivo delivery of a therapeutic agent, the carrier and therapeutic agent linked by a disulfide bond. According to U.S. Pat. No. 6,617,306, the carrier comprises a polymer, and at least one thiol compound conjugated to the polymer, such that the thiol group of the thiol compound and the thiol group of the therapeutic agent form a disulfide bond.

International Patent Application Publication No. WO 00/33888 teaches cleavable anti-tumor and anti-inflammatory compounds comprising a therapeutic agent capable of entering a target cell, an oligopeptide, a stabilizing group and an optional linker.

International Patent Application Publication No. 2005/072061 and U.S. Pat. Nos. 7,989,188 and 8,993,278 to some of the inventors of the present invention disclose compounds comprising a drug covalently linked to a functional group of an amino acid side chain, such compounds are useful for targeting drugs to neoplastic cells.

There remains an unmet need for methods of treating cancer which comprise administering to cancer patients compounds having antitumor activity but reduced cytotoxicity to normal tissues.

SUMMARY OF THE INVENTION

The present invention provides prodrugs comprising cytarabine conjugated to a single amino acid selected from the group consisting of aspartic acid, glutamic acid, asparagine, and glutamine, for use in treating neoplastic diseases.

The present invention is based in part on the unexpected discovery that administering a compound designated herein below Astarabine®, i.e., a conjugate of cytarabine and aspartic acid wherein cytarabine is covalently attached to the carboxyl group of the side chain of aspartic acid, to elderly patients having acute lymphocytic leukemia (ALL) or acute myeloid leukemia (AML), prolonged the survival of these patients.

It is known that the maximal standard of care dose of cytarabine that can be administered to patients of 75 or more years of age who have leukemia or lymphoma is 20 mg/m² of the subject's surface area. However, most of the patients at this age cannot tolerate even this low dose of cytarabine due to its severe side effects, and therefore are not treated with cytarabine at all. It is now disclosed for the first time that the prodrug Astarabine® administered to patients of 75 or more years of age having AML or ALL was safe and well tolerated at a daily dose of about 2 g/m² or even at higher doses. The prodrug Astarabine® was effective in attenuating or even eradicating newly diagnosed leukemia as well as secondary leukemia in elderly patients.

It is further disclosed that Astarabine® can be administered to elderly patients, i.e., 60 years old or older, at doses which are significantly higher (e.g., 5-30 times higher) than the maximal standard of care dose of cytarabine, and at such doses Astarabine® did not exert significant drug-related adverse effects during or post treatment.

According to one aspect, the present invention provides a method of treating a neoplastic disease, the method comprising administering to a subject in need of such treatment a pharmaceutical composition comprising a therapeutically effective amount of a compound, or a pharmaceutically acceptable salt thereof, having the general formula (I):

A-Cytarabine  (I)

wherein A denotes an amino acid residue, the amino acid is selected from the group consisting of aspartic acid, glutamic acid, asparagine and glutamine;

wherein cytarabine is attached to A through the side chain functional group of A; and

wherein the subject is a medically compromised subject who is not amenable to treatment with cytarabine.

According to one embodiment, A is aspartic acid residue and the compound is represented by the structure of formula (1), designated Astarabine®:

According to another embodiment, A is glutamic acid residue and the compound is represented by the structure of formula (2):

According to some embodiments, the pharmaceutically acceptable salt is a salt of an organic or inorganic acid or residue of an acid. According to additional embodiments, the acid is selected from the group consisting of acetic acid, hydrochloric acid, methanesulfonic acid, phosphoric acid, citric acid, lactic acid, succinic acid, tartaric acid, boric acid, benzoic acid, toluenesulfonic acid, benzenesulfonic acid, ascorbic acid, sulfuric acid, maleic acid, formic acid, malonic acid, nicotinic acid and oxalic acid. Each possibility represents a separate embodiment of the invention. According to one embodiment, the compound is Astarabine® and the pharmaceutically acceptable salt is acetate salt. According to another embodiment, the compound is Astarabine® and the pharmaceutically acceptable salt is hydrochloride salt.

According to additional embodiments, the neoplastic disease is selected from the group consisting of hematological cancers and non-hematological cancers. According to further embodiments, the hematological cancer is selected from the group consisting of leukemias, lymphomas, multiple myeloma, and Myelodysplastic Syndromes (MDS). Each possibility represents a separate embodiment of the invention.

According to yet further embodiments, the leukemia is selected from the group consisting of Acute Myeloid Leukemia (AML), Acute Lymphoblastic Leukemia (ALL), Chronic Myeloid Leukemia (CIVIL), and Chronic Lymphoblastic Leukemia (CLL). Each possibility represents a separate embodiment of the invention.

According to still further embodiments, the AML is selected from the group consisting of newly diagnosed AML, secondary AML, and relapsed/refractory AML. Each possibility represents a separate embodiment of the invention.

According to further embodiments, the lymphoma is selected from Hodgkin's Lymphoma and Non-Hodgkin's Lymphoma (NHL).

According to some embodiments, the MDS is selected from MDS with multilineage dysplasia (MDS-MLD), MDS with single lineage dysplasia (MDS-SLD), MDS with ring sideroblasts (MDS-RS), MDS with excess blasts (MDS-EB), MDS with isolated del(5q) and MDS unclassifiable (MDS-U). Each possibility represents a separate embodiment of the invention.

According to some embodiments, the medically compromised subject is selected from the group consisting of elderly subjects, subjects having hepatic dysfunction, subjects having renal dysfunction, subjects having pancreatic dysfunction, subjects having bone marrow dysfunction, subjects having cerebellar dysfunction, subjects having immunologic disorder, subjects having any other organ dysfunction which limits the use of cytarabine, subjects having relapsed or refractory hematological cancers, and any combination thereof. Each possibility represents a separate embodiment of the invention.

According to additional embodiments, the elderly subject is a subject of 50 or more years of age, such as of 60, 70, 75 or more years of age. Each possibility represents a separate embodiment of the invention.

According to further embodiments, Astarabine® is administered in a daily dosage of at least 2, 3, 5, 10, 15, 20, or at least 30 times greater than the maximal standard of care dose of cytarabine alone. Each possibility represents a separate embodiment of the invention.

According to yet further embodiments, Astarabine® is administered in a daily dose ranging from about 0.3 g/m² to about 10 g/m², such as in a daily dose of about 0.3 g/m², 0.5 g/m², 0.8 g/m², 1 g/m², 1.5 g/m², 2 g/m², 2.3 g/m², 2.5 g/m², 3 g/m², 3.5 g/m², 4 g/m², or 4.5 g/m² of the subject's surface area or any value in-between. Each possibility represents a separate embodiment of the invention.

According to some embodiments, the present invention provides a method for treating an acute myeloid leukemia (AML), an acute lymphocytic leukemia (ALL), a Chronic Myeloid Leukemia (CIVIL), a Chronic Lymphocytic Leukemia (CLL), a lymphoma, a myeloma, or a Myelodysplastic Syndrome (MDS) in a subject in need thereof, the method comprises administering to the subject a compound represented by the structure:

a pharmaceutically acceptable salt thereof; or a pharmaceutical composition comprising said compound or its pharmaceutically acceptable salt; wherein the therapeutically effective amount of said compound is administered at a daily dose of from 0.3 g/m² to 6 g/m² of the subject's surface area.

According to still further embodiments, the pharmaceutical composition is administered parenterally. According to further embodiments, the pharmaceutical composition is administered intravenously, intraperitoneally, intramuscularly, subcutaneously, intradermally, transdermally, or intravesicularly. Each possibility represents a separate embodiment of the invention. According to a certain embodiment, the pharmaceutical composition is administered intravenously. According to an exemplary embodiment, the pharmaceutical composition is administered by intravenous infusion for a period ranging from 15 minutes to 3 hours, such as for 30 minutes to one hour.

According to additional embodiments, the pharmaceutical composition is administered once a day for at least 3 days, such as for 3 days, 4, 5, 6, 8, 10, 12, or for 14 consecutive days or any integer in-between. According to further embodiments, the pharmaceutical composition is administered once a day for 6 consecutive days at least twice a month. According to yet further embodiments, the pharmaceutical composition is administered once every other day for at least one week, at least two weeks, three weeks or at least one month.

According to one exemplary embodiment, the compound is Astarabine® acetate, the subject is of at least 75 years of age having AML or ALL, and the pharmaceutical composition is administered at a daily dosage of at least two times greater than the maximal standard of care dose of cytarabine.

According to another exemplary embodiment, the compound is Astarabine® hydrochloride, the subject is of at least 75 years of age having AML or ALL, and the pharmaceutical composition is administered at a daily dosage of at least two times greater than the maximal standard of care dose of cytarabine.

According to another aspect, the present invention provides a method of treating a neoplastic disease, the method comprising administering to a subject in need of such treatment a pharmaceutical composition comprising a therapeutically effective amount of a compound, or a pharmaceutically acceptable salt thereof, represented by the structure of formula I:

A-Cytarabine  (I)

wherein A denotes the residue of an amino acid, the amino acid is selected from the group consisting of aspartic acid, glutamic acid, asparagine, and glutamine;

wherein cytarabine is attached to A through the side chain functional group of A; and

wherein adverse effects of the compound are reduced compared to the adverse effects of the non-conjugated cytarabine so that the compound can be administered in a dosage of at least two times greater than the maximal standard of care dose of cytarabine, without the subject experiencing dose limiting toxicity.

According to one embodiment, A is aspartic acid residue and the compound is represented by the structure of formula (1), designated Astarabine®:

According to another embodiment, A is glutamic acid residue and the compound is represented by the structure of formula (2):

According to some embodiments, the pharmaceutically acceptable salt is a salt of an organic or inorganic acid or residue of an acid. According to additional embodiments, the acid is selected from the group consisting of acetic acid, hydrochloric acid, methanesulfonic acid, phosphoric acid, citric acid, lactic acid, succinic acid, tartaric acid, boric acid, benzoic acid, toluenesulfonic acid, benzenesulfonic acid, ascorbic acid, sulfuric acid, maleic acid, formic acid, malonic acid, nicotinic acid and oxalic acid. Each possibility represents a separate embodiment of the invention. According to a certain embodiment, the compound is Astarabine® and the pharmaceutically acceptable salt is acetate salt. According to another embodiment, the compound is Astarabine® and the pharmaceutically acceptable salt is hydrochloride salt.

According to additional embodiments, the neoplastic disease is selected from the group consisting of hematological cancers and non-hematological cancers. According to further embodiments, the hematological cancer is selected from the group consisting of leukemias, lymphomas, multiple myeloma, and Myelodysplastic Syndromes (MDS). Each possibility represents a separate embodiment of the invention.

According to yet further embodiments, the leukemia is selected from the group consisting of Acute Myeloid Leukemia (AML), Acute Lymphoblastic Leukemia (ALL), Chronic Myeloid Leukemia (CIVIL), and Chronic Lymphoblastic Leukemia (CLL). Each possibility represents a separate embodiment of the invention.

According to still further embodiments, the AML is selected from the group consisting of newly diagnosed AML, secondary AML, and relapsed/refractory AML. Each possibility represents a separate embodiment of the invention.

According to further embodiments, the lymphoma is selected from Hodgkin's Lymphoma and Non-Hodgkin's Lymphoma (NHL).

According to some embodiments, the MDS is selected from MDS with multilineage dysplasia (MDS-MLD), MDS with single lineage dysplasia (MDS-SLD), MDS with ring sideroblasts (MDS-RS), MDS with excess blasts (MDS-EB), MDS with isolated del(5q) and MDS unclassifiable (MDS-U). Each possibility represents a separate embodiment of the invention.

According to some embodiments, the subject is a medically compromised subject who is not amenable to treatment with cytarabine. According to further embodiments, the subject is not amenable to treatment with standard-dose or high-dose cytarabine. According to further embodiments, the medically compromised subject is selected from the group consisting of elderly subjects, subjects having hepatic dysfunction, subjects having renal dysfunction, subjects having pancreatic dysfunction, subjects having bone marrow dysfunction, subjects having cerebellar dysfunction, subjects having immunologic disorder, subjects having any other organ dysfunction which limits the use of cytarabine, subjects having relapsed or refractory hematological cancers, and any combination thereof. Each possibility represents a separate embodiment of the invention.

According to additional embodiments, the elderly subject is a subject of 50 or more years of age, such as of 60, 70, 75 or more years of age. Each possibility represents a separate embodiment of the invention.

According to further embodiments, Astarabine® is administered in a daily dosage of at least 2 times to at least 30 times greater than the maximal standard of care dose of cytarabine alone, such as by 3, 5, 10, 15, 20 or 30 times greater. Each possibility represents a separate embodiment of the invention.

According to yet further embodiments, Astarabine® is administered in a daily dose ranging from about 0.3 g/m² to about 10 g/m², such as a daily dose of about 0.3 g/m², 0.5 g/m², 0.8 g/m², 1 g/m², 1.5 g/m², 2 g/m², 2.3 g/m², 2.5 g/m², 3 g/m², 3.5 g/m², 4 g/m², or 4.5 g/m² of the subject's surface area or any integer in-between. Each possibility represents a separate embodiment of the invention. According to other embodiments, the compound is administered at a daily dose of at least 0.3 g/m², 0.8 g/m², 1 g/m², 1.5 g/m², 2 g/m², 2.3 g/m², 2.5 g/m², 3 g/m², 4.5 g/m² or 6 g/m² of the subject's surface area.

According to still further embodiments, the pharmaceutical composition is administered parenterally. According to further embodiments, the pharmaceutical composition is administered intravenously, intraperitoneally, intramuscularly, subcutaneously, intradermally, transdermally, or intravesicularly. Each possibility represents a separate embodiment of the invention. According to a certain embodiment, the pharmaceutical composition is administered intravenously, preferably by infusion.

According to additional embodiments, the pharmaceutical composition is administered once a day for at least 3 days, such as for 3 days, 4, 5, 6, 8, 10, 12, or for 14 consecutive days or any integer in-between. According to further embodiments, the pharmaceutical composition is administered once a day for 6 consecutive days once or twice a month. According to yet further embodiments, the pharmaceutical composition is administered once every other day for at least one week, at least two weeks, three weeks or at least one month.

According to one exemplary embodiment, the compound is Astarabine® acetate and the pharmaceutical composition is administered at a daily dosage of at least two times greater than the maximal standard of care dose of cytarabine.

According to another exemplary embodiment, the compound is Astarabine® hydrochloride and the pharmaceutical composition is administered at a daily dosage of at least two times greater than the maximal standard of care dose of cytarabine.

According to a further aspect, the present invention provides a pharmaceutical composition comprising a compound, or a pharmaceutically acceptable salt thereof, represented by the structure of formula I:

A-Cytarabine  (I)

wherein A denotes an amino acid residue, the amino acid is selected from the group consisting of aspartic acid, glutamic acid, asparagine and glutamine; and

wherein cytarabine is attached to A through the side chain functional group of A;

for use in treating a neoplastic disease in a medically compromised subject who is not amenable to treatment with cytarabine according to the principles of the present invention.

According to a yet further aspect, the present invention provides a pharmaceutical composition comprising a compound, or a pharmaceutically acceptable salt thereof, for use in treating a neoplastic disease, the compound is represented by the structure of formula I:

A-Cytarabine  (I)

wherein A denotes the residue of an amino acid, the amino acid is selected from the group consisting of aspartic acid, glutamic acid, asparagine, and glutamine;

wherein cytarabine is attached to A through the side chain functional group of A; and

wherein adverse effects of the compound are reduced compared to the adverse effects of the non-conjugated cytarabine so that the compound being administered in a dosage of at least two times greater than the maximal standard of care dose of cytarabine, without the subject experiencing dose limiting toxicity.

These and other embodiments of the present invention will become apparent in conjunction with the figures, description and claims that follow.

BRIEF DESCRIPTION OF THE FIGURES

FIGS. 1A-B show in vivo measurements of maximal tolerated dose (MTD) of Astarabine®. In vivo tolerability/toxicology studies were used to determine the MTD of a single dose of Astarabine® in mice (FIG. 1A) or of 14 daily repeated doses of Astarabine® in mice (FIG. 1B). The MTD was evaluated for intravenous (IV) or intraperitoneal (IP) administration. The results are compared to MTD of cytarabine.

FIGS. 2A-B show the effect of Astarabine® on human leukemia growth in the hollow fiber model in transplanted nude mice in vivo. Leukemia model mice received 7 consecutive daily doses of one of the following treatments: Astarabine® in a dose of 6.25 mg/mouse/day, Astarabine® in a dose of 25 mg/mouse/day, Ara-C in a dose of 1.5 mg/mouse/day, or saline (control). In-vivo leukemia growth was measured. FIG. 2A shows the growth of Molt-4 leukemia cells. FIG. 2B shows the growth of CCRF-CEM leukemia cells.

DETAILED DESCRIPTION OF THE INVENTION

The present invention provides methods of treating a neoplastic disease comprising administering to medically compromised patients, particularly elderly patients of 75 or more years of age, a conjugate of cytarabine covalently linked to a single amino acid, such patients typically cannot be treated with the non-conjugated cytarabine due to its severe adverse effects, and thus are given supportive therapy only. The present invention fulfills a long-felt need for treating medically compromised patients, particularly elderly patients, who have been diagnosed as having hematological cancers, yet cannot be treated with cytarabine. The conjugates of the present invention enable treatment of these cancer patients with cytarabine at doses that would have been toxic if administered in its non-conjugated form.

Definitions

The term “medically compromised” subjects as used herein refers to a sub-population of subjects who are weakened or impaired medically so that they cannot tolerate the non-conjugated cytarabine due to its severe adverse effects. Medically compromised subjects include, but are not limited to, subjects suffering from or having renal dysfunction, hepatic dysfunction, pancreatic dysfunction, bone marrow dysfunction, cerebellar, dysfunction, immunologic disorder, any other organ, tissue or system dysfunction which limits the use of cytarabine, and a combination thereof.

The term “non-conjugated cytarabine” as used herein refers to cytarabine or an analog or derivative thereof which is free and not covalently attached to an amino acid.

The terms “renal dysfunction”, “hepatic dysfunction”, “pancreatic dysfunction”, “bone marrow dysfunction” and “cerebellar dysfunction” refer to a state in which the organ/tissue function, e.g., kidney, liver, pancreas, bone marrow, and cerebellum, is decreased relative to a normal state. In general, organ/tissue dysfunction is a state characterized in that any one or more measurement values of inspection items for organ function are deviated from the range of normal values (reference values).

The terms “maximal standard of care dose” and “the recommended maximal dose” of cytarabine are used herein interchangeably and refer to the dosage, e.g., the daily dose, of cytarabine approved by the U.S. FDA for administration to a human subject, which dosage does not cause unacceptable adverse effects and is dependent on the subject's age and physical condition so that a subject of 50 or less years of age can be typically treated with a daily dose of cytarabine of up to 3 g/m², a subject of 50 to 60 years of age can be typically treated with a daily dose of cytarabine of up to 1.5 g/m², a subject of 60 to 75 years of age can be typically treated with a daily dose of cytarabine ranging from 0.1 g/m² to 0.5 g/m², and a subject of 75 or more years of age can be treated with a daily dose of cytarabine of up to 20 mg/m² of the subject's surface area. However, it should be noted that most of the subjects of 75 or more years of age cannot be treated with cytarabine at all due to its severe adverse effects.

The term “dose limiting toxicity” is defined in accordance with the Common Terminology Criteria of Adverse Events Version 3.0 (CTCAE). Dose limiting toxicity occurs upon administration of a compound to a subject if any of the following events are observed within a drug treatment cycle: Grade 4 neutropenia (i.e., absolute neutrophil count (ANC)≤500 cells/mm³) for 5 or more consecutive days or febrile neutropenia (i.e., fever≤38.5° C. with an ANC≤1000 cells/mm³); Grade 4 thrombocytopenia (i.e., ≤25,000 cells/mm³ or bleeding episode requiring platelet transfusion); Grade 4 fatigue, or a two-point decline in ECOG performance status; Grade 3 or greater nausea, diarrhea, vomiting, and/or myalgia despite the use of adequate/maximal medical intervention; Grade 3 or greater non-hematological toxicity (except fatigue); retreatment delay of more than 2 weeks due to delayed recovery from toxicity related to treatment with the compound; Grade 2 or greater cardiac toxicity of clinical significance (e.g., a decline in the resting ejection fraction to 40%-≤50% or shortening fraction to 15%-≤24%; cardiac troponin T≥0.05 ng/mL).

The term “therapeutically effective amount” of the compound is that amount of the compound which is sufficient to provide a beneficial effect to the subject to which the compound is administered. An effective amount of the compound may vary according to factors such as the disease state, age, sex, and weight of the individual.

The terms “treatment”, “treat”, “treating” and the like, are meant to include slowing, arresting or reversing the progression of a disease. These terms also include alleviating, ameliorating, attenuating, eliminating, or reducing one or more symptoms of a disease, even if the disease is not actually eliminated and even if progression of the disease is not itself slowed or reversed. A subject refers to a mammal, preferably a human being.

The term “residue of a drug” refers to a drug excluding the functional group that is used to attach the amino acid for the formation of the amino acid-drug conjugate A-D. Similarly, the term “residue of an amino acid” refers to an amino acid excluding the functional group that is used to attach the drug for the formation of the amino acid-drug conjugate A-D.

The term “about” in reference to a numerical value stated herein is to be understood as the stated value+/−10%.

The amino acids used in this invention are those which are available commercially or are available by routine synthetic methods. When there is no indication, either the L or the D isomer may be used.

According to one aspect, the present invention provides a method of treating a neoplastic disease, the method comprising administering to a medically compromised subject who is not amenable to treatment with cytarabine a pharmaceutical composition comprising a therapeutically effective amount of a compound, or a pharmaceutically acceptable salt thereof, having the general formula (I):

A-Cytarabine  (I)

wherein A denotes an amino acid residue, the amino acid is selected from the group consisting of aspartic acid, glutamic acid, asparagine and glutamine; and

wherein cytarabine is attached to A through the side chain functional group of A.

The term “pharmaceutically acceptable salt” of a drug refers to a salt according to IUPAC conventions. Pharmaceutically acceptable salt is an inactive ingredient in a salt form combined with a drug. The term “pharmaceutically acceptable salt” as used herein refers to salts of the compounds of the general formula (I), formula (II), e.g., compounds (1) and (2), or any other salt form encompassed by the generic formulae which are substantially non-toxic to living organisms. Typical pharmaceutically acceptable salts include those salts prepared by reaction of the compounds of the present invention with a pharmaceutically acceptable mineral, base, acid or salt. Acid salts are also known as acid addition salts (see herein below). Pharmaceutically acceptable salts are known in the art (Stahl and Wermuth, 2011, Handbook of pharmaceutical salts, Second edition).

According to some embodiments of the present invention, the amino acid can have free non-modified amino and carboxyl termini, or one or both of the amino and carboxyl termini can be modified. The compound of the present invention can thus be represented by the general formula II:

A′ denotes the side chain of an amino acid, said amino acid is selected from the group consisting of aspartic acid, glutamic acid, asparagine and glutamine; D denotes the residue of cytarabine or an analog or derivative thereof;

R¹, R² and R² are each independently selected from a group consisting of a hydrogen and a lower alkyl; and

X is selected from the group consisting of a carboxyl, an amide and a hydrazide.

According to preferred embodiments, R1, R2 and R3 are each a hydrogen.

According to another preferred embodiment, X is a carboxyl group.

According to a certain embodiment, R1, R2 and R3 are each a hydrogen and X is a carboxyl.

According to some embodiments, X is an amide group present as a carboxy amide.

Analogs of cytarabine include, but are not limited to, N⁴-behenoyl ara-C, N⁴-Palmitoyl-ara-C, 2′-Azido-2′-deoxy ara-C, 5′-(Cortisone 21-phosphoryl) ester of ara-C, 5′-Acyl esters of ara-C, N⁴ Behenoyl-ara-C, ara-C conjugate with poly-H⁵ (2-hydroxyethyl)-L-glutamine, Dihydro-5-azacytidine, 5-Aza-arabinosylcytosine and 5-Aza 2′-deoxycytidine.

According to some embodiments, the pharmaceutically acceptable salt of the compound of the invention is represented by the general formula (III):

A-D·Y  (III)

wherein A is the amino acid residue, the amino acid is selected from the group consisting of aspartic acid, glutamic acid, asparagine and glutamine;

D is cytarabine or an analog or derivative thereof, and

Y is a pharmaceutically acceptable organic or inorganic acid or residue of an acid.

According to some embodiments, Y is a pharmaceutically acceptable acid selected from the group consisting of acetic acid, hydrochloric acid, methanesulfonic acid, phosphoric acid, citric acid, lactic acid, succinic acid, tartaric acid, boric acid, benzoic acid, toluenesulfonic acid, benzenesulfonic acid, ascorbic acid, sulfuric acid, maleic acid, formic acid, malonic acid, nicotinic acid and oxalic acid. Each possibility represents a separate embodiment of the present invention.

According to exemplary embodiments, the salt form of the conjugate Astarabine® is acetate or hydrochloride.

Without wishing to be bound to any theory or mechanism of action, the amino-acid-cytarabine conjugates of the present invention are transported into the cancer cells via amino acid transporters thereby bypassing multi-drug resistance (MDR) mechanisms, and within the cells these conjugates are cleaved to release cytarabine which arrests cell growth or kill the cell. As free cytarabine and free cytarabine metabolites were detected in cancer cells, the conjugates of the present invention act as pro-drugs.

Pharmaceutical Compositions

The present invention provides pharmaceutical compositions comprising at least one of the compounds of the present invention and a pharmaceutically acceptable carrier or diluent, optionally further comprising one or more excipients.

The term “pharmaceutically acceptable” means approved by a regulatory agency of the Federal or a state government or listed in the U. S. Pharmacopeia or other generally recognized pharmacopeia for use in animals, and more particularly in humans.

The term “carrier” refers to a diluent, adjuvant, excipient, or vehicle with which the therapeutic compound is administered. Such pharmaceutical carriers can be sterile liquids, such as water and oils, including those of petroleum, animal, vegetable or synthetic origin, such as peanut oil, soybean oil, mineral oil, sesame oil and the like, polyethylene glycols, glycerin, propylene glycol or other synthetic solvents.

For intravenous administration of a therapeutic compound, water is a preferred carrier. Saline solutions and aqueous dextrose and glycerol solutions can also be employed.

According to a certain embodiment, the formulation of Astarabine® for intravenous administration is an aqueous isotonic solution having osmolarity of about 300 mOsm and a pH of 4-8. Thus, the pharmaceutically acceptable carrier of Astarabine® can be a buffered saline solution, a buffered dextrose solution, or a buffered glycerol solution having osmolarity of about 300 mOsm and a pH of 4-8.

The buffer of Astarabine® solution can be a pharmaceutically acceptable mono-ionic buffer system or a poly-ionic buffer system having an ionization pK in the range of 4-8.

Various buffers having a pK of 4-8 can be employed for adjusting the pH of Astarabine® solution such as, for example, ACES (N-(acetamido)-2-aminoethansulfonic acid); Acetatate; N-(2-acetamido)-2-iminodiacetic acid; BES (N,N-bis[2-hydroxyethyl]-2-aminoethansulfonic acid); Bicine (2-(Bis(2-hydroxyethyl)amino)acetic acid); Bis-Tris methane (2-[Bis(2-hydroxyethyl)amino]-2-(hydroxymethyl)propane-1,3-diol); Bis-Tris propane (1,3-bis(tris(hydroxymethyl)methylamino)propane); Carbonate; Citrate; 3,3-dimethyl glutarate; DIPSO (3-[N,N-bis(2-hydroxyethyl)amino]-2-hydroxypropansulfonic acid); N-ethylmorpholine; Glycerol-2-phosphate; Glycine; Glycine-amid; HEPBS (N-(2-hydroxyethyl)piperazin-N′-4-buthanesulfonic acid); HEPES (N-(2-hydroxyethyl)piperazin-N′-2-ethanesulfonic acid); HEPPS (N-(2-hydroxyethyl)piperazin-N′-(3-propanesulfonic acid)); HEPPSO (N-(2-hydroxyethyl)piperazin-N′-(2-hydroxypropanesulfonic acid); Histidine; Hydrazine; Imidazole; Maleate; 2-methylimidazole; MES (2-(N-morpholino)ethanesulfonic acid); MOBS (4-(N-morpholino)-butansulfonic acid); MOPS (3-(N-morpholino)-propanesulfonic acid; MOPSO (3-(N-morpholino)-2-hydroypropanesulfonic acid); Oxalate; Phosphate; Piperazine; PIPES (1,4-Piperazine-diethanesulfonic acid); POPSO (Piperazine-N,N′-bis(2-hydroxypropanesulfonic acid)); Succinate; Sulfite; TAPS (3-[[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]amino]propane-1-sulfonic acid); TAPSO (3-[[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]amino]-2-hydroxypropane-1-sulfonic acid); Tartaric acid; TES (2-[[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]amino]ethanesulfonic acid); THAM (Tris) (2-Amino-2-hydroxymethyl-propane-1,3-diol); and Tricine (N-(2-Hydroxy-1,1-bis(hydroxymethyl)ethyl)glycine).

According to some embodiments, the buffer is a sulfonic acid derivative buffer including, but not limited to, ACES, BES, DIPSO, HEPBS, HEPES, HEPPS, HEPPSO, MES, MOBS, MOPS, MOPSO, PIPES, POPSO, Sulfite, TAPS, TAPSO, and TES buffer.

According to additional embodiments, the buffer is a carboxylic acid derivative buffer including, but not limited to, Acetatate, N-(2-acetamido)-2-iminodiacetic acid, 2-(Bis(2-hydroxyethyl)amino)acetic acid, Carbonate, Citrate, 3,3-dimethyl glutarate, Lactate, Maleate, Oxalate, Succinate, and Tartaric acid buffer.

According to further embodiments, the buffer is an amino acid derivative buffer including, but not limited to, Bicine, Glycine, Glycine-amid, Histidine, and Tricine buffer.

According to yet further embodiments, the buffer is a phosphoric acid derivative buffer including, but not limited to, Glycerol-2-phosphate and phosphate buffer.

Alternatively, the buffered saline for Astarabine® formulation can be, for example, Hank's balanced salt solution, Earle's balanced salt solution, Gey's balanced salt solution, HEPES buffered saline, phosphate buffered saline, Plasma-lyte, Ringer's solution, Ringer Acetate, Ringer lactate, Saline citrate, or Tris buffered saline.

The buffered dextrose solution for Astarabine® formulation can be, for example, acid-citrate-dextrose solution or Elliott's B solution.

According to exemplary embodiments, the solutions for injection of Astarabine® is Plasma-Lyte A or Compound Sodium Lactate purchased from Baxter.

The compositions can take the form of solutions, suspensions, emulsion, tablets, pills, capsules, powders, sustained-release formulations and the like. The composition can be formulated as a suppository, with traditional binders and carriers such as triglycerides, microcrystalline cellulose, gum tragacanth or gelatin.

The pharmaceutical composition can further comprise pharmaceutical excipients including, but not limited to, sodium chloride, potassium chloride, magnesium chloride, sodium gluconate, sodium acetate, calcium chloride, sodium lactate, and the like. The composition, if desired, can also contain minor amounts of sugar alcohols, wetting or emulsifying agents, and pH adjusting agents. Antibacterial agents such as benzyl alcohol or methyl parabens; antioxidants such as ascorbic acid or sodium bisulfite; chelating agents such as ethylenediaminetetraacetic acid; and agents for the adjustment of tonicity such as sodium chloride or dextrose are also envisioned.

Pharmaceutical compositions for parenteral administration can also be formulated as suspensions of the active compounds. Such suspensions may be prepared as oily injection suspensions or aqueous injection suspensions. For oily suspension injections, suitable lipophilic solvents or vehicles can be used including fatty oils such as sesame oil, or synthetic fatty acids esters such as ethyl oleate, triglycerides or liposomes. Aqueous injection suspensions may contain substances which increase the viscosity of the suspension, such as sodium carboxymethyl cellulose, sorbitol or dextran. Optionally, the suspension may also contain suitable stabilizers or agents which increase the solubility of the compounds, to allow for the preparation of highly concentrated solutions.

For transmucosal and transdermal administration, penetrants appropriate to the barrier to be permeated may be used in the formulation. Such penetrants, including for example DMSO or polyethylene glycol, are known in the art.

For oral administration, the compounds can be formulated readily by combining the active compounds with pharmaceutically acceptable carriers and excipients well known in the art. Such carriers enable the compounds of the invention to be formulated as tablets, pills, dragees, capsules, liquids, gels, syrups, slurries, suspensions, and the like, for oral ingestion by a subject. Pharmacological preparations for oral use can be made using a solid excipient, optionally grinding the resulting mixture, and processing the mixture of granules, after adding suitable auxiliaries if desired, to obtain tablets or dragee cores. Suitable excipients are, in particular, fillers such as sugars, including lactose, sucrose, mannitol, or sorbitol; cellulose preparations such as, for example, maize starch, wheat starch, rice starch, potato starch, gelatin, gum tragacanth, methyl cellulose, hydroxypropylmethyl-cellulose, sodium carbomethylcellulose; and/or physiologically acceptable polymers such as polyvinylpyrrolidone (PVP). If desired, disintegrating agents may be added, such as cross-linked polyvinyl pyrrolidone, agar or alginic acid or a salt thereof such as sodium alginate.

In addition, enteric coating can be useful if it is desirable to prevent exposure of the compounds of the invention to the gastric environment.

Pharmaceutical compositions which can be used orally include push-fit capsules made of gelatin as well as soft, sealed capsules made of gelatin and a plasticizer, such as glycerol or sorbitol. The push-fit capsules may contain the active ingredients in admixture with filler such as lactose, binders such as starches, lubricants such as talc or magnesium stearate and, optionally, stabilizers.

In soft capsules, the active compounds may be dissolved or suspended in suitable liquids, such as fatty oils, liquid paraffin, or liquid polyethylene glycols. In addition, stabilizers may be added.

Pharmaceutical compositions of the present invention may be manufactured by processes well known in the art, e.g., by means of conventional mixing, dissolving, granulating, grinding, pulverizing, dragee-making, levigating, emulsifying, encapsulating, entrapping or lyophilizing processes.

The dosage of a composition to be administered will depend on many factors including the subject being treated, the stage of cancer, the route of administration, and the judgment of the prescribing physician.

Therapeutic Use

The present invention provides a method of treating a neoplastic disease or a viral disease comprising administering to a subject in need of such treatment a pharmaceutical composition comprising a therapeutically effective amount of a compound having the general formula (I), (II), e.g. compounds (1) or (2) or a pharmaceutically acceptable salt thereof, as described herein above, and a pharmaceutically acceptable carrier.

The neoplastic disease can be selected from hematological cancers or non-hematological cancers.

Hematological cancers include leukemias, lymphomas, myelomas, and Myelodysplastic Syndromes (MDS) including, but not limited to, myeloid leukemia, lymphocytic leukemia, e.g., acute myeloid leukemia (AML), chronic myeloid leukemia (CML), acute lymphocytic leukemia (ALL), chronic lymphocytic leukemia (CLL), Hodgkin's lymphoma, Non-Hodgkin's lymphoma, multiple myeloma, and Waldenstrom's macroglobulinemia.

The term “Myelodysplastic Syndromes” (MDS) refers to a heterogeneous group of hematopoietic malignancies characterized by blood cytopenias, ineffective hematopoiesis and a hypercellular bone marrow. The MDSs are preleukemic conditions in which transformation into acute myeloid leukemia (AML) occurs in approximately 30-40% of cases. Unless allogenic stem cell transplantation can be offered, MDS is generally considered to be an uncurable condition.

Non-hematological cancers also known as solid tumors include, but are not limited to, sarcoma, carcinoma, fibrosarcoma, myxosarcoma, liposarcoma, chondrosarcoma, osteogenic sarcoma, chordoma, angiosarcoma, endotheliosarcoma, mesothelioma, Ewing's tumor leiomydsarcoma, rhabdomyosarcoma, squamous cell carcinoma, basal cell carcinoma, adenocarcinoma, sweat gland carcinoma, sebaceous gland carcinoma, papillary carcinoma, papillary adenocarcinoma, cystadenocarcinoma, medullary carcinoma, bronchogenic carcinoma, renal cell carcinoma, hepatoma bile duct carcinoma, choriocarcinoma, seminoma, embryonal carcinoma, Wilms' tumor cervical cancer, testicular tumor, lung carcinoma, small cell lung carcinoma, bladder carcinoma, epithelial carcinoma, astrocytoma, Kaposi's sarcoma, and melanoma. Each possibility represents a separate embodiment of the invention.

Non-hematological cancers include cancers of organs, wherein the cancer of an organ includes, but is not limited to, breast cancer, bladder cancer, colon cancer, rectal cancer, endometrial cancer, kidney cancer, lung cancer, cervical cancer, pancreatic cancer, prostate cancer, testicular cancer, thyroid cancer, ovarian cancer, brain cancer including ependymoma, glioma, glioblastoma, medulloblastoma, craneopharyngioma, pinealoma, acustic neuroma, hemangioblastoma, oligodendroglioma, menangioma, neuroblastoma, retinoblastoma, and their metastasis. Each possibility represents a separate embodiment of the invention.

The present invention further provides a method for the treatment of an infection caused by a viral agent that is a cancer-causing virus. Thus, the invention provides a method for the treatment of a viral infection caused by a viral oncogene. Non-limiting examples of such viruses include human papillomavirus, Hepatitis B, Hepatitis C, Epstein-Barr virus, Human T-lymphotropic virus, Kaposi's sarcoma-associated herpesvirus, and Merkel cell polyomavirus. Each possibility represents a separate embodiment of the invention.

A viral disease can be caused by other viruses including, but not limited to, human immunodeficiency virus (HIV), herpes simplex virus (HSV), cytomegalovirus (CMV), and varicella zoster virus (VZV). Each possibility represents a separate embodiment of the invention. According to one embodiment, the viral disease is Herpes viral encephalitis.

The method of the present invention can be useful for treating a neoplastic disease in a subject having an immunological disease or disorder. Immunological diseases or disorders include, but are not limited to, rheumatoid arthritis (RA), psoriatic arthritis, systemic lupus erythematosus (SLE), lupus nephritis, Inflammatory bowel disease (IBD), irritable bowel syndrome, type I diabetes, immune thrombocytopenic purpura, multiple sclerosis, Sjorgren's syndrome, Hashimoto's thyroiditis, Grave's disease, primary biliary cirrhosis, Wegener's granulomatosis, tuberculosis, and Waldenstrom's macroglobulemia.

The method of the present invention can be useful for treating a neoplastic disease in subjects having organ dysfunction, such as hepatic dysfunction, renal dysfunction, pancreatic dysfunction, bone marrow dysfunction, and cerebellar dysfunction.

The term “hepatic dysfunction” refers to a state in which the liver function is decreased relative to a normal state. In general, hepatic dysfunction is a state characterized in that any one or more measurement values of inspection items for liver function (e.g. levels of blood AST, ALT, ALP, TTT, ZTT, total bilirubin, total protein, albumin, lactate dehydrogenase, choline esterase and the like) are deviated from the range of normal values (reference values). Hepatic dysfunction is characteristic of diseases such as, for example, fulminant hepatitis, chronic hepatitis, viral hepatitis, alcoholic hepatitis, hepatic fibrosis, liver cirrhosis, hepatic cancer, autoimmune hepatitis, drug allergic hepatopathy, and primary biliary cirrhosis.

Renal dysfunction is characteristic of diseases such as, for example, acute renal failure, glomerulonephritis, chronic renal failure, azotemia, uremia, immune renal disease, acute nephritic syndrome, rapidly progressive nephritic syndrome, nephrotic syndrome, Berger's Disease, chronic nephritic/proteinuric syndrome, tubulointerstital disease, nephrotoxic disorders, renal infarction, atheroembolic renal disease, renal cortical necrosis, malignant nephroangiosclerosis, renal vein thrombosis, renal tubular acidosis, renal glucosuria, nephrogenic diabetes insipidus, Bartter's Syndrome, Liddle's Syndrome, polycystic renal disease, interstitial nephritis, acute hemolytic uremic syndrome, medullary cystic disease, medullary sponge kidney, hereditary nephritis, and nail-patella syndrome.

Pancreatic dysfunction is characteristic of diseases such as, for example, diabetes, hyperglycemia, impaired glucose tolerance, and insulin resistance.

Bone marrow dysfunction is characteristic of diseases such as, for example, osteomyelitis, dyshematopoiesis, ion deficiency anemia, pernicious anemia, megaloblastosis, hemolytic anemia, and aplastic anemia.

Cerebellar dysfunction is characteristic of motor and neuro-behavioral disorders such as, for example, hypotonia, dysarthria, dysmetria, dysdiadochokinesia, impaired reflex, and intention tremor.

The pharmaceutical compositions of the invention may be administered by any suitable administration route selected from the group consisting of parenteral and oral administration routes. According to some embodiments, the route of administration is via parenteral administration. In various embodiments, the route of administration is intravenous, intraarterial, intramuscular, subcutaneous, intraperitoneal, intracerebral, intracerebroventricular, intrathecal or intradermal administration route. For example, the pharmaceutical compositions can be administered systemically, for example, by intravenous (i.v.) or intraperitoneal (i.p.) injection or infusion. According to a certain embodiment, the pharmaceutical composition is administered by intravenous infusion for 30 minutes to 2 hours, such as for 1 hour. The compositions of the invention may be administered locally and may further comprise an additional active agent and/or excipient.

Toxicity and therapeutic efficacy of the compounds described herein can be determined by standard pharmaceutical procedures in cell cultures or experimental animals, e. g., by determining the IC50 (the concentration which provides 50% inhibition of cell growth) and the MTD (Maximal tolerated dose in tested animals) for a subject compound. The data obtained from cell culture assays and animal studies can be used in formulating a range of dosage for use in human subjects. The exact formulation, route of administration and dosage can be chosen by the individual physician in view of the patient's condition (See e.g., Fingl, et al., 1975, in “The Pharmacological Basis of Therapeutics”, Ch. 1 pp. 1).

The compound, e.g. Astarabine®, can be administered in a daily dose ranging from about 0.3 g/m² to about 10 g/m² of the subject's surface area. According to some embodiments, the compound, e.g., Astarabine®, can be administered at a daily dose ranging from about 0.5 g/m² to about 5 g/m² of the subject's surface area. According to some embodiments, the compound can be administered at a daily dose ranging from about 0.5 g/m² to about 4.5 g/m² of the subject's surface area. According to other embodiments, the compound, e.g., Astarabine®, is administered at a daily dose of about 0.3, 0.5, 0.8, 1, 1.5, 2, 2.3, 2.5, 3, 3.5, 4, 4.5, 5, 6, 7, 8, 9, 10 g/m² of the subject's surface area. Each possibility represents a separate embodiment of the invention. According to other embodiments, the compound is administered at a daily dose of at least 0.3 g/m², 0.8 g/m², 1 g/m², 1.5 g/m², 2 g/m², 2.3 g/m², 2.5 g/m², 3 g/m², 4.5 g/m² or 6 g/m² of the subject's surface area.

According to some embodiments, the present invention provides a method for treating an acute myeloid leukemia (AML), an acute lymphocytic leukemia (ALL), a Chronic Myeloid Leukemia (CML), a Chronic Lymphocytic Leukemia (CLL), a lymphoma, a myeloma, or a Myelodysplastic Syndrome (MDS) in a subject in need thereof, the method comprises administering to the subject a compound represented by the structure:

a pharmaceutically acceptable salt thereof; or a pharmaceutical composition comprising said compound or its pharmaceutically acceptable salt; wherein the therapeutically effective amount of said compound is administered at a daily dose of from 0.3 g/m² to 6 g/m² of the subject's surface area. According to some embodiments, Astarabine® is administered by intravenous infusion at a daily dose ranging from 0.3 g/m² to 4.5 g/m² of the subject's surface area. According to some embodiments, the pharmaceutical composition is administered at least once a month. According to additional embodiments, the pharmaceutical composition is administered at least twice a month. According to further embodiments, the pharmaceutical composition is administered at least once a week. According to yet further embodiments, the pharmaceutical composition is administered at least twice a week. According to still further embodiments, the pharmaceutical composition is administered once a day for at least one week. According to further embodiments, the pharmaceutical composition is administered at least once a day for at least one week or until the subject is cured.

According to some embodiments, the pharmaceutical composition is administered once a day for at least 2, 3, 4, 5, 6, 8, 10, 12, or at least 14 consecutive days once a month. Alternatively, the pharmaceutical composition is administered once a day for at least 2, 3, 4, 5, 6, or 12 days twice a month, or further alternatively the pharmaceutical composition is administered every day or twice a week until the patient is cured.

According to some embodiments, the compound is administered at least once daily, for a period of 3-6 days. According to some other embodiments, the compound is administered at least once daily for a period of at least 3 days. According to some other embodiments, the compound is administered at least once daily for a period of 4 days. According to some other embodiments, the compound is administered at least once daily for a period of 5 days. According to some other embodiments, the compound is administered at least once daily for a period of 6 days. According to some other embodiments, the compound is administered every other day, for a period of 3-6 days. According to some other embodiments, the compound is administered every other day for a period of at least 3 days. According to some other embodiments, the compound is administered every other day for a period of 4 days. According to some other embodiments, the compound is administered every other day for a period of 5 days. According to some other embodiments, the compound is administered every other day for a period of 6 days.

In some embodiments, where the pharmaceutical composition is used for preventing recurrence of cancer, the pharmaceutical composition may be administered regularly for prolonged periods of time according to the clinician's instructions.

In some cases it may be advantageous to administer a large loading dose followed by periodic (e.g., weekly) maintenance doses over the treatment period. The compounds can also be delivered by slow-release delivery systems, pumps, and other known delivery systems for continuous infusion. Dosing regimens may be varied to provide the desired circulating levels of a particular compound based on its pharmacokinetics. Thus, doses are calculated so that the desired circulating level of a therapeutic agent is maintained.

Typically, the effective dose is determined by the activity and efficacy of the compound and the condition of the subject as well as the body weight or surface area of the subject to be treated. The dose and the dosing regimen are also determined by the existence, nature, and extent of any adverse side effects that accompany the administration of the compounds in a particular subject. According to some embodiments, the therapeutically effective amount of the compound is administered daily. According to some other embodiment, the therapeutically effective amount of the compound is administered every other day.

The following examples are to be considered merely as illustrative and non-limiting in nature. It will be apparent to one skilled in the art to which the present invention pertains that many modifications, permutations, and variations may be made without departing from the scope of the invention.

Example 1 Effect of Astarabine® on Different Cell Lines

The effect of Astarabine® on different cell lines was evaluated. Briefly, various cell lines were obtained from ATCC or ECACC. Hematological cells were grown in RPMI medium containing 10-20% FBS and 1% glutamine. Solid tumor cells were grown in DMEM medium containing 10-20% FBS and 1% glutamine. Cells were seeded into 96-well plates, 50,000 cells/ml, 0.2 ml per well. Test substances were diluted in saline or PBS and added in final concentrations of 0.1 nM to 10 μM, in a volume of 20 μl. The study was conducted in triplicates, PBS was used as control. Plates were incubated for 72 hr at 37° C., 5% CO₂. At the end of the exposure period, a MTT assay using the MTT reagent [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] was performed. MTT was added to each well at a concentration of 5 mg/ml in a volume of 0.02 ml. Plates were incubated at 37° C. for 3 h. The plates were centrifuged at 3500 rpm for 5 minutes and the supernatant was aspired. The pellets which contained MTT crystals were each dissolved in 0.2 ml DMSO. Absorbance was determined using ELISA reader at a wavelength of 570 nm.

The results are summarized in Table 1.

TABLE 1 IC₅₀ values of Astarabineg ® vs. cytarabine in tumor cell lines. Cytarabine IC₅₀ IC₅₀ in Cell line Cell type Units Astarabine ® cytarabine literature Molt-4 Human nM  4.0-24.0 1.1-12.3   29 ± 1.8^(*1) acute lympho- blastic leukemia HL-60 Human nM 255.7-276.2 49.6-165.2   37 ± 6.1^(*2) promyelo- cytic leukemia CCRF-SB Human μM   11-21.4 1.9-3.1  4.2^(*3) acute lympho- blastic leukemia K562 Human nM 194.0-516.0 46.1-380.6 chronic myelo- genous leukemia RPMI8226 Human μM 33.4-144  9.7-63   myeloma CCRF- Human nM 23.3-40.8 3.1-25.2 30^(*3) CEM Caucasian acute lympho- blastic leukemia T lympo- blastoid line THP-1 Human μM 7.1-52 2.3-5.5  monocytic leukemia SU DHL-1 Human nM 314-335 124-524  large cell lymphoma Kasumi-1 Human μM 7.6 No acute response myelo- blastic leukemia MEG 01 Human μM 1.7 1.2-5.6  chronic myelo- genous leukemia SU DHL-5 Human B- nM 196 323 cell non Hodgkin's lymphoma RS 4:11 Human nM 27.1 26.4 acute lympho- blastic leukemia P388.D1 Mouse μM 1.9-2.6 0.6-0.9  lymphoid macro- phage L1210 Mouse nM  39.4-116.4 12.2-16.4  40 ± 9^(*4) DBA/2 lympho- cytic leukemia HepG2 Human μM  7-7.5 0.98-1.16  0.185 ± 0.24^(*5) hepato- cellular carcinoma NCIH727 Human μM 1.3-2.8 0.59-0.77  lung non small cell carcinoma A2780 Human nM 457.4 72.0-113.8 14 ± 4^(*6) ovarian carcinoma HT29 Human μM No No colon response response adenocar- cinoma LOVO Human μM No No colon response response adenocar- cinoma ^(*1)—Ogbomo et al., Neoplasia 10(12): 1402-1410, 2008; ^(*2)—Qin et al., Clin, Cancer Res. 13(14): 4225-4232, 2007; ^(*3)—Manfredini et al., Bioorg. Med. Chem. 8: 539-547, 2000; ^(*4)—Breistol et al., Cancer Res. 59: 2944-2949, 1999; ^(*5)—Groveet al., Cancer Res. 55: 3008-3011, 1995; ^(*6)—Ruiz Van Haperen, Cancer Res. 54: 4138-4143, 1994.

The results demonstrated that most of the hematological cancer cell lines assayed were sensitive to Astarabine®, while solid tumor cell lines were less sensitive.

Astarabine® metabolite assay in human leukemia cell lines detected free cytarabine metabolites, indicating that Astarabine® is a pro-drug of cytarabine.

Example 2

Maximal tolerated dose and efficacy of Astarabine® in mice Maximal tolerated dose (MTD) of Astarabine® injected once or for multiple injections intrperitoneally (IP) or intravenously (IV).

Single Dose IP:

Ten weeks of age IRC mice were injected IP with a single dose of Astarabine®, ranging from 1428 to 8271 mg/kg (50 to 300 mg/mice, respectively). Clinical evaluation included mobility observations, food and water consumption. Mice in all groups showed normal behavior. After 7 days, the mice were sampled for hematology and biochemistry and then subjected to necropsy.

Blood samples obtained from mice injected with the high dose of Astarabine® (8271 mg/kg) showed normal results after 7 days of recovery. In all mice, all tissues were indicated as normal, with no macroscopic findings. Concentration of 8271 mg/kg Astarabine® administrated by IP route was considered as MTD of Astarabine® single dose IP acute toxicity.

Repeated Dose IP:

Astarabine® was administrated IP to TRC mice for 7 days in elevated dosages from 156 to 781 mg/kg/day (5 to 25 mg/mouse/day, respectively).

All mice were inspected daily during drug administration and recovery period. Clinical evaluation included mobility observations, food and water consumption. Mice in all groups showed normal behaviour during the administration and recovery periods. Hematology and biochemical blood tests were shown normal at the end of the experiment. Gross necropsy showed no abnormal findings.

Concentration of 781 mg/kg/day Astarabine® administrated IP for 7 days, a dose which is accumulative dose of 5467 mg/kg, was considered as the MTD (maximal tolerated dose) in mice.

Single Dose IV:

IRC mice were injected once IV with Astarabine® in a dose ranging from 1000 to 8000 mg/kg. The mice were evaluated for 14 days. The results indicated that Astarabine® at a dose of 8000 mg/kg was tolerated by both male and female ICR mice. The following parameters: clinical signs, body weight, food consumption and blood analysis, were normal for both male and female mice at this dose, i.e., 8000 mg/kg. There was no drug dependent death in this dose level. It is therefore concluded that 8000 mg/kg is the MTD of Astarabine® in mice for a single IV administration.

Repeated Dose IV:

IRC mice were injected with Astarabine® IV daily for 14 days in a dosage ranging from 400 mg/kg/day to 1200 mg/kg/day. Based on the results of this 14 days intravenous repeated dose study in mice, it was concluded that the IV maximal tolerated dose for Astarabine® is 400 mg/kg/day, administrated for 14 consecutive days. The total administered dose in this group was 5600 mg/kg. All measured parameters such as clinical observations, neurobehavioral observations, motor activity observations, body weight, food consumption, blood analysis and urine analysis, were within the normal range as compared to the non-treated group. Thus, Astarabine® in a concentration of 400 mg/kg/day was considered as the NOAEL (No Adverse Effect Level) in mice. In vivo tolerability/toxicology studies to determine the MTD of a single dose in mice are shown in FIG. 1A and of repeated doses in mice are shown in FIG. 1B.

Next, the efficacy of Astarabine® in vivo was studied on a human leukemia (Molt-4 and CCRF-CEM cells) hollow fiber model transplanted in nude mice. Astarabine® was injected at doses of 6.25 mg/mouse/day and 25 mg/mouse/day intraperitoneally (IP), daily, for 7 consecutive days; cytarabine was injected at a dose of 1.5 mg/mouse/day. Leukemia cell growth was measured using the MTT assay as described in Example 1 herein above.

The results showed that Astarabine® at a dose of 6.25 mg/mouse/day and 25 mg/mouse/day or cytarabine at a dose of 1.5 mg/mouse/day inhibited the growth of Molt-4 cells by 76.9%, 82.8% and 81.1%, respectively, in the in-vivo hollow fiber Molt-4 leukemia model. Similarly, Astarabine® at a dose of 6.25 mg/mouse/day and 25 mg/mouse/day or cytarabine at a dose of 1.5 mg/mouse/day inhibited the growth of CCRF-CEM cells by 71.9%, 72.0% and 73.3%, respectively, in the in-vivo CCRF-CEM leukemia model. Thus, these results show a therapeutic efficacy of Astarabine® against CCRM-CEM and Molt-4 human leukemia cells. The efficacy of Astarabine® was similar to that of cytarabine. FIG. 2A shows the response in the Molt-4 leukemia model. FIG. 2B shows the response in the CCRF-CEM leukemia model.

The results indicate that Astarabine® improves drug tolerability and reduces toxicity in animals by 10-20 fold compared to the reported toxicity of cytarabine, while maintaining its anti-cancer activity. Hence, Astarabine® can serve as a safer, non-toxic alternative to cytarabine for the treatment of various leukemias.

Example 3 Astarabine Formulation and Administration

The drug Astarabine® was supplied as a sterile lyophilized powder in glass ampoules of 1 g per ampoule. The drug was dissolved in 10 ml of sterile water for injection to obtain a final concentration of Astarabine® of 100 mg/ml. Following complete dissolution in water, the drug was further diluted in an injection/infusion solution. The administered dose was calculated in g/m² according to the patient's age and medical condition.

A. Drug Dosage of 0.5 g/m²;

The delivery dosage for the patient was calculated according to the following formula: Drug dosage in g/m²×Body Surface Area (BSA) of the patient in m²=Dosage administered to a patient in grams (g).

0.5 g/m²×1.72 m²=0.86 g (860 mg).  Calculation example:

Thus, a volume of 8.6 ml (860 mg) from the 100 mg/ml Astarabine® solution were added to 500 ml of sterile buffered saline for injection, e.g., Ringer lactate, 273 mOsm/L, pH=6.5. The Astarabine® formulation was administered to the patient by infusion over 1 hour.

B. Drug Dosage of 4.5 g/m²,

4.5 g/m²×1.65 m²=7.425 g  Calculation example:

A volume of 74.25 ml (7.425 g) from the 100 mg/ml Astarabine® solution were added to 500 ml of sterile buffered saline for injection, e.g., Plasma-lyte-A, 294 mOsm/L, pH=7.4, and were administered to the patient by infusion over 1 hour.

Example 4 Efficacy of Astarabine® in Elderly Patients

A clinical study was conducted to evaluate the performance and safety of Astarabine® in AML and ALL patients.

Study Design

Phase I/IIa, open-label, uncontrolled, single-center study enrolled patients of 18 or more years of age with relapsed or refractory acute leukemia or those unfit for intensive therapy, as judged by the treating physician. The study was approved by the Rambam IRB (approval #0384-11).

Patients were enrolled into 4 Astarabine® escalating dose cohorts, each included 3 patients. Treatment was administered as a 1-hour single daily infusion for 6 consecutive days.

Astarabine® doses for each infusion:

-   -   For age ≤50 years: 0.5 g/m², 1.5 g/m², 3 g/m², 4.5 g/m²     -   For age >50 years: 0.3 g/m², 0.8 g/m², 1.5 g/m², 2.3 g/m²

Results

The outcome of 10 patients is presented in Table 2. Nine patients had AML, of whom five patients had refractory/relapsed AML and four patients had newly diagnosed secondary AML unfit for intensive therapy. One patient had newly diagnosed ALL. Median age was 80 years.

At the end of a 10 month period: Four patients were alive, two of whom were in continuous complete remission (CR) at 7 and 9 months post treatment. Four patients died from disease progression, one died suddenly 7 days post treatment, an event that was postulated to be treatment unrelated. No significant adverse effects were recorded during or post therapy apart from neutropenic fever.

TABLE 2 Clinical results of treating elderly patients with Astarabine ®. BM BLASTS Follow- Patient Astarabine Day Day Day up in No. Age Dose Diagnosis 0 14 30 Outcome months 1 75 0.3 Refractory 100%  90%  83% Died- 3 gr/m²/day AML DP 2 81 0.3 Refractory 100%  64%  70% Died- 2 gr/m²/day AML DP 3 27 0.5 Refractory  90%  37%  60% Died- 6 gr/m²/day AML DP 4 76 0.8 Secondary N/D  39%  63% Died- 4 gr/m²/day AML DP 5 81 0.8 Secondary  80%   5%   0% Alive in 9 gr/m²/day AML CR¹ 6 63 0.8 Refractory  85% 100% 100% Died- 1 gr/m²/day AML DP 7 90 1.5 ALL  89%   3%  0.2% Alive in 7 gr/m²/day CR 8 86 1.5 Secondary  63%  80%   8% Alive in 6 gr/m²/day AML PR 9 80 1.5 Secondary 100% N/A N/A Died 1 gr/m²/day AML 10 63 2.3 Relapsed 100% N/A N/A Died 1 gr/m²/day AML * No significant drug-related adverse effects were observed. PR—partial remission; CR—complete remission; DP—disease progression; ¹relapsed after 9 months in CR; being considered for another Astarabine ® cycle.

The results suggest that Astarabine®, a pro-drug of cytarabine, is safe and very well tolerated, even for patients of 80 or more years of age. Remarkably, Astarabine® administration resulted in remission in three out of ten patients having acute leukemia, and this compound was particularly efficacious in patients who were newly diagnosed with leukemia.

Example 5 Phase 2, Open-Label, Single Arm, Multi-Center Study to Assess the Efficacy and Safety of Astarabine® as a Single Agent in Adults Unfit for Intensive Chemotherapy with Relapsed or Refractory Acute Myeloid Leukemia or Higher-Risk Myelodysplastic Syndromes

A clinical study is conducted to assess the efficacy, and safety of Astarabine® in patients unfit for intensive chemotherapy with AML or HR MDS that failed or relapsed following first line therapy.

Study Design

This is a prospective, phase 2, open-label, multi-center, single arm, single agent study, in unfit adult patients with AML or Higher-risk MDS (HR MDS) who failed or relapsed following first-line therapy.

The study consists of three periods: Screening: Up to 28 days. Treatment: Recurrent 6 days treatment courses with Astarabine®. Follow-up: The period of time from last day of Astarabine® treatment to completion of one year (365 days±7 days) from the first day of Astarabine® treatment. Post-study Follow-up: One-Year follow-up of survival, starting at the end of study visit.

Treatment Period:

Eligible patients are receiving the first induction course with Astarabine®, 4.5 g/m²/d administered IV over 1 hour for 6 consecutive days. The first day of the induction is defined as Study Day 1. Following the first treatment course:

1. AML patients in complete remission (CR) or CR with incomplete count recovery (CRi) or CR with partial hematologic recovery (CRh), and HR MDS patients with CR are receiving between 2 to 4 maintenance courses of 6-day treatment with Astarabine®, every 4-6 weeks from first dose of previous treatment course. The Astarabine® dose in these subsequent treatment courses will be 2.3 or 4.5 g/m²/d. The reduced dose must be used in case of previous courses toxicity and is allowed in certain cases according to physician discretion following consultation with the study medical monitor. The interval between treatment courses may be extended to up to 12 weeks (from first dose of previous treatment course) to allow resolution of toxicities per investigator discretion. 2. Patients with stable disease defined as failure to achieve at least PR, but with no evidence of disease progression or patients in partial response (PR) are receiving a second 6-day course with Astarabine®, at a dose of 4.5 g/m²/d. Following which:

-   -   a. AML patients in PR or CR, (including CR, CRh or CRi) and HR         MDS patients in PR or CR are treated with maintenance courses as         detailed above;     -   b. Patients in stable disease or disease progression discontinue         the participation in the study.

Investigational Product

Dose and route of administration: Astarabine® should be administered IV over 1 hour for 6 consecutive days.

The Astarabine® dose in the first treatment course is 4.5 g/m²/d. The first treatment course should be administered while patients are hospitalized.

The Astarabine® dose of the consecutive treatment courses is 4.5 or 2.3 g/m²/d.

Treatment courses except for the first one, can be administered on an outpatient basis.

Study Duration

The total duration for each participating patient is up to 52 weeks (365 days) in addition to a screening period of up to 28 days.

Efficacy Outcome Measures Primary Endpoint: For MDS Patients:

Overall response rate (ORR), defined as the proportion of patients who achieve a CR or PR per proposal for modification of the International Working Group (IWG) criteria for MDS, 2006. (Cheson B D. et al. Clinical application and proposal for modification of the International Working Group (IWG) response criteria in myelodysplasia. Blood. 2006 Jul. 15; 108(2):419-25. doi: 10.1182/blood-2005-10-4149. Epub 2006 Apr. 11. PMID: 16609072, incorporated herein by reference). For AML patients: CR Rate, defined as the proportion of patients who achieve a CR per the IWG 2006 Criteria (Ayalew Tefferet et al, International Working Group (IWG) consensus criteria for treatment response in myelofibrosis with myeloid metaplasia, for the IWG for Myelofibrosis Research and Treatment (IWG-MRT). Blood 2006; 108 (5): 1497-1503, incorporated herein by refference). CR is defined as BM blasts <5%, absence of circulating blasts and blasts with Auer rods, absence of extramedullary disease, ANC≥1.0×10⁹/L (1,000/μL); platelet count ≥100×10⁹/L (100,000/μL).

Secondary Endpoints: For MDS Patients:

1. Overall improvement rate (OIR), defined as the proportion of patients reaching a CR, Marrow CR, PR, or hematologic improvement (HI) per proposal for modification of the IWG criteria for MDS, 2006. Marrow CR is defined as bone marrow blasts ≤5% and decreased by 50% over pretreatment. Peripheral blood: if HI responses, they will be noted in addition to marrow CR. HI is defined as:

-   -   a. Erythroid response (pretreatment, <11 g/dL) is defined as Hgb         increase by ≥1.5 g/dL. Relevant reduction of units of red blood         cells (RBC) transfusions by an absolute number of at least 4 RBC         transfusions/8 weeks, compared with the pretreatment transfusion         number in the previous 8 weeks. Only RBC transfusions given for         a Hgb of ≤9.0 g/dL will count in the RBC transfusion response         evaluation.     -   b. Platelet response (pretreatment <100×10⁹/L) is defined as         absolute increase of ≥30×10⁹/L for patients starting with         >20×10⁹/L platelets, and an increase from <20×10⁹/L to >20×10⁹/L         and by at least 100%.     -   c. Neutrophil response (pretreatment, <1.0×10⁹/L) is defined as         at least 100% increase and an absolute increase >0.5×10⁹/L.         2. Duration of Response (DOR), defined as time from the date of         the first observed PR/CR to the date of the first subsequent         documented disease progression or relapse per IWG 2006 criteria,         or death from any cause.         3. Progression Free Survival (PFS), for patients with at least a         PR, defined as time from the date of the first dose of study         treatment to the date of the first documented disease         progression or relapse per IWG 2006 criteria, or death from any         cause.         4. Overall Survival (OS), defined as time from the date of the         first dose of study treatment to the date of death from any         cause.         5. Rate of bone marrow blast response, defined as the proportion         of patients with a reduction in bone marrow blast counts         following treatment.         6. Time to AML transformation, defined as time from first         treatment dose to the first date in which AML is established.         7. CR Rate, defined as the proportion of participants who         achieved a CR per the IWG 2006 Criteria.         8. Improvement in cytopenia, including:     -   a. Rate of PLT transfusion independence, defined as the         proportion of patients who become platelet         transfusion-independent.     -   b. Rate of RBC transfusion independence, defined as the         proportion of patients who become RBC transfusion-independent.     -   c. Rate of cytogenetic response, defined as the proportion of         patients with cytogenetic response per the IWG 2006 Criteria.         9. Rate of HI, defined as the proportion of patients reaching a         HI per the IWG 2006 Criteria.

For AML Patients:

1. Overall response rate (ORR) including; CR (MRD+, MRD−), CRh, and CRi according to the Diagnosis and Management of AML in Adults: 2017 ELN Recommendations from an International Expert Panel Revised (Dohner et al., Diagnosis and management of AML in adults: 2017 ELN recommendations from an international expert panel. Blood. 2017 Jan. 26; 129(4):424-447. doi: 10.1182/blood-2016-08-733196. Epub 2016 Nov. 28. PMID: 27895058; PMCID: PMC5291965, incorporated herein by reference).

-   -   a. CRh is defined as CR criteria except for partial         hematological recovery (CRh) rate defined as all CR criteria         except for neutrophils ≥0.5×10⁹/L (500/μL) and thrombocytes         ≥50×10⁹/L (50,000/μL).     -   b. CRi is defined as all CR criteria except for residual         neutropenia (<1.0×10⁹/L (1,000/μL)) or thrombocytopenia         (<100×10⁹/L (100,000/μL)).         2. Duration of Response (DOR), defined as time from the date of         the first observed CR/CR+CRh/CRh/CRi to the date of the first         subsequent documented disease progression or relapse per IWG         2006 criteria, or death from any cause.         3. Progression Free Survival (PFS) for patients with at least         CRi, defined as time from the date of the first dose of study         treatment to the date of the first documented disease         progression or relapse per IWG 2006 criteria, or death from any         cause.         4. Overall Survival (OS) defined as time from the date of the         first dose of study treatment to the date of death from any         cause.         5. Rate of bone marrow blast response defined as percentages of         participants with a reduction in bone marrow blast counts.         6. Rate of CR without Minimal Residual Disease (CR-MRD), defined         as the proportion of patients reaching a CR with BM blast         negativity by multi-color flow cytometry.         7. Time to neutrophil recovery in patients with CR or PR,         defined as:     -   a. Number of days from Day 1 of commencing induction therapy to         first day of neutrophils 0.5×10⁹/L.     -   b. Number of days from Day 1 of commencing induction therapy to         first day of neutrophils 1×10⁹/L.         8. Time to platelet recovery in patients with CR or PR, defined         as:     -   a. Number of days from Day 1 of commencing induction therapy to         first day of platelets 50×10⁹/L.     -   b. Number of days from Day 1 of commencing induction therapy to         first day of platelets 100×10⁹/L.         9. Rate of patients who become platelet transfusion-independent,         defined as the proportion of patients who become platelet         transfusion-independent based on the comparison of the PLT         transfusion requirements in the 8 weeks prior to study Day 1 to         the transfusion requirements in the 8 weeks following the last         Astarabine treatment course.         10. Rate of patients who become red blood cell (RBC)         transfusion-independent, defined as the proportion of patients         who become RBC transfusion-independent based on the comparison         of the RBC transfusion requirements in the 8 weeks prior to         study Day 1 to the transfusion requirements in the 8 weeks         following the last Astarabine® treatment course.         It is appreciated by persons skilled in the art that the present         invention is not limited by what has been particularly shown and         described hereinabove. Rather the scope of the present invention         includes both combinations and sub-combinations of various         features described hereinabove as well as variations and         modifications. Therefore, the invention is not to be constructed         as restricted to the particularly described embodiments, and the         scope and concept of the invention will be more readily         understood by references to the claims, which follow. 

1. A method for treating an acute myeloid leukemia (AML), an acute lymphocytic leukemia (ALL), a Chronic Myeloid Leukemia (CVL), a Chronic Lymphocytic Leukemia (CLL), a lymphoma, a myeloma, or a Myelodysplastic Syndrome (MDS) in a subject in need thereof, the method comprises administering to the subject a compound represented by the structure:

a pharmaceutically acceptable salt thereof; or a pharmaceutical composition comprising said compound or its pharmaceutically acceptable salt; wherein the therapeutically effective amount of said compound is administered at a daily dose of from 0.3 g/m² to 6 g/m² of the subject's surface area.
 2. The method of claim 1, wherein the compound is administered at a daily dose of at least 0.3 g/m², 0.8 g/m², 1 g/m², 1.5 g/m², 2 g/m², 2.3 g/m², 2.5 g/m², 3 g/m², 4.5 g/m² or 6 g/m² of the subject's surface area.
 3. The method of claim 1, wherein the compound is administered at least once daily for a period of at least 3 days.
 4. The method of claim 1, wherein the therapeutically effective amount of the compound is administered daily.
 5. The method of claim 1, wherein the therapeutically effective amount of the compound is administered every other day.
 6. The method of claim 1, wherein the compound is administered as a pharmaceutically acceptable salt of an organic or inorganic acid selected from the group consisting of acetic acid, hydrochloric acid, methanesulfonic acid, phosphoric acid, citric acid, lactic acid, succinic acid, tartaric acid, boric acid, benzoic acid, toluenesulfonic acid, benzenesulfonic acid, ascorbic acid, sulfuric acid, maleic acid, formic acid, malonic acid, nicotinic acid and oxalic acid.
 7. The method of claim 6, wherein salt is hydrochloric acid.
 8. The method of claim 1, wherein the AML is a newly diagnosed AML, a secondary AML, or relapsed/refractory AML.
 9. The method of claim 1, wherein the MDS is MDS with multilineage dysplasia (MDS-MLD), MDS with single lineage dysplasia (MDS-SLD), MDS with ring sideroblasts (MDS-RS), MDS with excess blasts (MDS-EB), MDS with isolated del(5q) or MDS unclassifiable (MDS-U).
 10. The method of claim 1, wherein the administration is parenteral, intravenous or by intravenous infusion.
 11. The method of claim 10, wherein the administration is intravenous infusion for a period ranging from 15 minutes to 3 hours,
 12. The method of claim 1, wherein the subject is a medically compromised subject who is not amenable to treatment with cytarabine.
 13. The method of claim 1, wherein the subject is not amenable to treatment with standard-dose or high-dose cytarabine, or is a subject with hepatic dysfunction, a subject with renal dysfunction, a subject with pancreatic dysfunction, a subject with bone marrow dysfunction, a subject with cerebellar dysfunction, a subject having an immunologic disorder, a subject with a relapsed or refractory hematological cancer, or any combination thereof. 